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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
placental insufficiency
Summary
- Definition
- A placenta disease that is characterized by insufficient blood flow to the placenta during pregnancy.
- Super Class
- placenta disease
External Links
- Disease Ontology
- DOID:3891
- Mondo Disease Ontology
- MeSH
- UMLS
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 79053 | ALG8 | ALG8 alpha-1,3-glucosyltransferase | |
| 79087 | ALG12 | ALG12 alpha-1,6-mannosyltransferase | |
| 79679 | VTCN1 | V-set domain containing T cell activation inhibitor 1 | |
| 79868 | ALG13 | ALG13 UDP-N-acetylglucosaminyltransferase subunit | |
| 91949 | COG7 | component of oligomeric golgi complex 7 | |
| 145173 | B3GLCT | beta 3-glucosyltransferase | |
| 201595 | STT3B | STT3 oligosaccharyltransferase complex catalytic subunit B |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q12860 | Contactin-1 | |
| Q12918 | Killer cell lectin-like receptor subfamily B member 1 | |
| Q13085 | Acetyl-CoA carboxylase 1 | |
| Q13563 | Polycystin-2 | |
| Q15392 | Delta(24)-sterol reductase | |
| Q15485 | Ficolin-2 | |
| Q16831 | Uridine phosphorylase 1 | |
| Q16836 | Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial | |
| Q5H8A4 | GPI ethanolamine phosphate transferase 2 | |
| Q6NSJ0 | Myogenesis-regulating glycosidase |
